Variant report

Variant	rs9849526
Chromosome Location	chr3:157072169-157072170
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11919151	0.85[CEU][hapmap];0.87[JPT][hapmap]
rs13064292	0.85[CEU][hapmap]
rs16827528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66928005	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7632367	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9845182	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157056200-157072600	Weak transcription	HUVEC	blood vessel
2	chr3:157057000-157072800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:157066000-157073200	Weak transcription	HSMM	muscle
4	chr3:157066000-157076400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:157066000-157086800	Weak transcription	Pancreas	Pancrea
6	chr3:157066600-157076000	Weak transcription	NH-A	brain
7	chr3:157066600-157083200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr3:157066800-157072200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr3:157066800-157074000	Weak transcription	NHLF	lung
10	chr3:157068400-157072600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr3:157070200-157072400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:157070400-157073400	Enhancers	NHDF-Ad	bronchial
13	chr3:157070400-157077400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:157070800-157073200	Enhancers	Osteobl	bone
15	chr3:157071200-157073400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr3:157071600-157073400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:157072000-157072600	Enhancers	K562	blood
18	chr3:157072000-157074800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:157072000-157074800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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